Canonical Allele Identifier:
CA1665449777
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.134398878C= , CM000668.2:g.134398878C= | GRCh38 |
| NC_000006.11:g.134720016C= , CM000668.1:g.134720016C= | GRCh37 |
| NC_000006.10:g.134761709C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_428023.2:n.23+149C= |